Module 3 Flashcards

Brain Development & Genetics

1
Q

DNA

A

2 strands of a sequence of 4 chemical bases (ATCG)
- bases on one strand pair with complementary bases on other

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2
Q

genes

A
  • sections of DNA that code for specific proteins
    • about 20,000 different genes
    • only -1% of our total DNA
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3
Q

regulatory DNA regulates genes

A

switch on and off throughout life
- some on/off built in, but some can be influenced by environment (thalidomide)
- on/ off can malfunction, creating regulator-gene defects

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4
Q

chromosomes

A

contain our DNA, 23 pairs
- 22 pairs of autosomes
- 1 pair are sex chromosomes- y much smaller (fewer genes): contains gene that sets in motion processes for creating males

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5
Q

random assortment

A

during meiosis one of each of the 23 pairs of chromosomes randomly goes to new egg or sperm- en up with new combinations of chromosomes in offspring
- diversity at the level of whole chromosomes

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6
Q

crossing over

A

during meiosis two member of a pair of chromosomes sometimes swap sections of DNA to random assortment
- diversity within chromosomes

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7
Q

mutations

A

random changes in DNA
- mostly bad, so often die out

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8
Q

alleles

A

different variants of the same gene that we inherit from each of our parents (one on each chromosome)
- only about 1/3 of genes have these
- the gene for eye color can have different alleles (brown, blue, green)
- blood types are alleles
- we can be homozygous or heterozygous
- if heterozygous, dominant allele is expressed over recessive (e.g. your brown eye-color alleles are BrBl)
- recessive: only affected if you inherit gene from both parents
- dominant: affected if you inherit gene from one parents
- fun fact: green eye color is recessive to brown, but dominant to blue

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9
Q

co-dominant and incomplete dominance

A
  • codominant alleles= both expressed (AB blood)
  • incomplete dominance alleles= blend of alleles (hair shape)
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10
Q

genotype vs. phenotype

A
  • genotype is your genetic information (genes, particular alleles)
  • phenotype is the way your genetic info is expressed
    • your actual outcomes: eye color, height, IQ, personality, and everything else
    • influenced by environment
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11
Q

norm of reaction

A
  • all the phenotypes that could theoretically occur from given genotype across all possible environments
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12
Q

gene-environmental interaction

A
  • one’s genes make them particularly sensitive or susceptible to particular environments
    • e.g., phenylketonuria (PKU): genetic inability to metabolize amino acid phenylalanine
      • causes severe mental retardation
      • with a strict diet, you’re fine
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13
Q

methylation

A

methyl molecule binds to DNA; impacts typically reduces gene expression

  • more methylation= less stress regulation= bad
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14
Q

heritability

A

variability in a trait in the population that is attributable to genes
- differs across populations who may have greater or lower environmental impact

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15
Q

genetic influence on developmental outcomes (like cognitive abilities) ….

A

increases over time!
- why?
- 1. new genetic effects as maturation unfolds
- for instance, genes that are only active during puberty
- 2. genetic tendency to seek out particular environments magnifies effects of genetic differences

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16
Q

two kinds of environmental influences

A
  • shared = how the environment makes you more like your siblings (SES, school, etc)
  • non-shared = how the environment makes you unlike your siblings (anything that happens to you but not your siblings)
    • as you age, you experience more and more non-shared environment
17
Q

phenotype is the results of

A

genetics+ how the environment makes you the same + how the environment makes you different

18
Q

parts of a neuron

A
  • cell body: contains basic biological material that keeps neuron functioning
  • dendrites: receive input from other cells and conducts toward the cell body
  • axon: conducts electrical signals to connections with other neurons
19
Q

synaptogenesis

A

connections between neurons formed btw dendrites and axon terminals

20
Q

apoptosis (cell death) and synaptic pruning

A
  • way to many connections at first
    • cell death and elimination of unneeded/ unused connections
    • neurons that fire together, wire together
      • neural darwinism
    • problems with pruning linked to diseases like autism (too little) and schizophrenia (too much)
21
Q

experience-expectant plasticity

A

reasonably typical environment will fine-tune neural circuitry in a normal way, makes us largely similar to each other
- visual system: just need to see some things
- efficient! means fewer genes can be devoted to normal development
- but also vulnerable to aberrant input
- strabismus and other visual issues need correcting early or brain will permanently reorganize (timing matters)
- if normal experience is lacking, or if brain injury occurs, all is not lost, the brain can often reorganize and compensate:
- deaf individuals have language areas tuned to visual info
- blind individuals show activation in visual areas when reading braille

22
Q

experience-dependent plasticity

A

brain development as a function of individual experience
- not what everyone tends to experience
- violinists, braille readers have increased cortical space dedicated to fingers
- dyslexia therapy can change your brain
- rats growing in impoverished, normal, or complex environments

23
Q

low SES infants have

A
  • smaller brain volumes
    • thinner cortices
    • lower ERP power